Tag: fda recall
Arrow recalls percutaneous thrombolytic device kits over risk of separation
Arrow International has recalled its Arrow-Trerotola over-the-wire 7Fr percutaneous thrombolytic device (PTD) kits, which are used to remove clots in adult patients who have...
FDA recalls SoloPath vascular access system following reports of malfunction
The US Food and Drug Administration have issued a Class I Recall of the SoloPath (Terumo Medical) ballon-expandable transfemoral system and re-collapsible balloon access...
